Inhibition of Aspartate Aminotransferase by Glycation In Vitro Under Various Conditions

Incubation of 50 mM d -glucose with aspartate aminotransferase (AST, EC 2.6.1.1) preparations (purified pig heart enzyme or a rat liver 20,000 × g supernatant) at 25°C had no effect on enzyme activity. 50 mM d -fructose or d -ribose gradually inhibited pig heart AST under the same conditions to zero activity after 14 days. 50 mM dl -glyceraldehyde decreased enzyme activity to zero after 6 days of incubation. The inhibition of pig heart AST by 50 mM d -fructose or d -ribose was marked even at a temperature of 4°C but it was less pronounced than at 25°C. There was no effect of 0.5 mM 2-oxoglutarate on AST activity during incubation, while the presence of 25 mM l -aspartate decreased it rapidly. 0.5 mM 2-oxoglutarate partly prevented inhibition of AST by d -ribose or d -fructose, while an analogous experiment with 25 mM aspartate resulted in a rapid decline similar to that in the absence of sugars.     

Fine structure of Lasaea subviridis and Mysella tumida sperm (Bivalvia,Galeommatacea)

Summary Lasaea subviridis and Mysella tumida sperm resemble the primitive spermatozoan type, but exhibit several unique morphological features. L. subviridis sperm heads vary in shape and size owing to differing degrees of nuclear condensation. A fully mature, heterogenous acrosomal vesicle with an associated axial rod is present. Up to 50% of L. subviridis sperm in developing gonads have conspicuously angled flagella that propel the sperm cells in irregular helical paths. This may represent a penultimate stage in sperm development because the remainder of the sperm cells have posteriorly-directed flagella and swim in a nonhelical anterior direction. A trend toward a reduction in both nuclear condensation and swimming ability may be a long-term consequence of increasing degrees of localized, but non-internal self-fertilization in marine invertebrates that brood. Mysella tumida sperm are monomorphic and possess numerous microvilli (30–60 nm in diameter and up to 5.7 m in length) that resemble stereocilia and radiate from the cell membrane surrounding the basal body. In this species, the sperm cell does not have an axial rod, and the complex acrosomal vesicle contains five distinct zones of varying electron opacity. One of these zones is a transverse, electron-opaque band that is apparently composed of rolled-up membrane. Following acrosomal breakdown, this membrane unfolds to cover the anterior tip of the sperm cell. Although both L. subviridis and M. tumida are hermaphroditic, the relative size of their male investments is conspicuously different. Approximately 40–50% of the M. tumida gonadal volume is testis compared with about 5% of that in L. subviridis.     

Histocompatibility Gene Organization and Mixed Lymphocyte Reaction

TRANSFORMATION of allogenic lymphocytes in mixed cultures depends chiefly on an incompatibility between the lymphocyte donors at the major histocompatibility locus in man (HL-A), mouse (H-2) and rat (H-l)¹. Although the mouse H-2 locus can be divided into several regions each of which controls one or more antigenic specificities² and two or more subloci control HL-A antigens in man³, it is not known whether all parts of the major histocompatibility locus are equally important in eliciting transformation in mixed lymphocyte cultures. We now show that capacity to elicit lymphocyte transformation is different for different parts of the mouse H-2 locus.     

The extent and differences in mitotic activity of the root tip ofVicia faba L.

Mitotic activity does not stop for different meristematic cells of the root apex at the same distance from the initials. The differences are connected with the functional heterogeneity of the apical meristem of the root. The arrangement of vascular bundles,i.e. the alternation of independent xylem and phloem groups, is of major importance. In broad bean roots, the protophloem sieve elements stop dividing first. The centre of the stelei. e. late metaxylem elements stop dividing next. Division in the stele gradually ceases centrifugally, while it ceases centripetally in the peripheral part of the root. The cylindrical region with prolonged cell division includes internal layers of the cortex including endodermis, pericycle and adjoining cells of the stele. Proximally apical meristem is reduced to isolated strands of cells adjacent to the protoxylem poles. Pericycle cells stop dividing last at a distance of approx. 9–10 mm from the initials. The number of the division cycles is limited and is specific for individual cell types. Epidermal and cortical cells divide in broad bean roots transversely approximately seven times, cells of late metaxylem approximately five times. Root apical meristem is an asynchronous cell population with a different duration of the mitotic cycle. We determined local variations in the duration of the mitotic cycle in the apical meristem of broad bean root by means of colchicine-induced polyploidy. The cells of the quiescent centre had the longest mitotic cycle after colchicine treatment. The region of the proper root adjacent to the quiescent centre was mixoploid (2n and 4n). Isolated cells with a long cycle occurred also in the cortex and in the central cylinder. Cells with a division cycle of 18h were found in the root cap, in the epidermis, in the cortex and in the central cylinder. Relatively numerous cells with the shortest division cycle, approx. 12 h, occurred farther of the quiescent centre in the epidermis, in the cortex, in the pericycle, and in adjacent layers of the stele through-out the entire meristematic region. The results derived from the analysis of the apical meristem are discussed in connection with the ontogenesis of different types of cells taking part in the primary structure of the root.     

Inorganic self-organisation in precambrian cherts

Silica biomorphs are inorganic self-organized precipitates resulting from a crystal aggregation process controlled by a metal silicate membrane. They display morphological and symmetric properties of living organisms and form under physico-chemical conditions similar to some geochemical conditions suggested for the chemical precipitation of Precambrian chert precursors. In consequence, these inorganic precipitates are proposed as an alternative interpretation to be considered when trying to decipher the biogenicity of putative Precambrian microbiotas.